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J Org Chem ; 76(11): 4669-74, 2011 Jun 03.
Article in English | MEDLINE | ID: mdl-21526866

ABSTRACT

Stepwise, selective DIBAL reduction of the acetonide diester derived from tartaric acid followed by the Horner-Emmons reaction effectively provided desymmetrized hydroxy mono-olefination products in a one-pot operation.


Subject(s)
Dioxolanes/chemistry , Organometallic Compounds/chemistry , Tartrates/chemistry , Catalysis , Esters , Oxidation-Reduction
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